Primary Device ID | 08714729191797 |
NIH Device Record Key | 0ed8ede5-3a6d-4283-9c17-926d02157049 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Flexima™ APDL |
Version Model Number | M001281350 |
Company DUNS | 021717889 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729191797 [Primary] |
FFA | TUBE, DRAINAGE, SUPRAPUBIC |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2024-01-03 |
Device Publish Date | 2016-09-24 |
08714729323976 | Drainage Catheter System Kit with Dissolving Tip |
08714729323969 | Drainage Catheter System with Dissolving Tip |
08714729323501 | Drainage Catheter System Kit |
08714729323495 | Drainage Catheter System Kit |
08714729323488 | Drainage Catheter System Kit |
08714729323471 | Drainage Catheter System Kit |
08714729323150 | Drainage Catheter System |
08714729323143 | Drainage Catheter System |
08714729323112 | Drainage Catheter System |
08714729323105 | Drainage Catheter System |
08714729323099 | Drainage Catheter System |
08714729323082 | Drainage Catheter System |
08714729323044 | Drainage Catheter System |
08714729300694 | Drainage Catheter System Kit |
08714729300670 | Drainage Catheter System |
08714729191827 | Drainage Catheter System with Dissolving Tip |
08714729191797 | Drainage Catheter System with Dissolving Tip |
08714729191780 | Drainage Catheter System with Dissolving Tip |
08714729191759 | Drainage Catheter System |
08714729127970 | Drainage Catheter System with Dissolving Tip |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLEXIMA 85498974 5003555 Live/Registered |
B. Braun Medical S.A.S. 2011-12-19 |
FLEXIMA 79062629 not registered Dead/Abandoned |
B. BRAUN MEDICAL SAS 2008-10-08 |
FLEXIMA 78726747 3139010 Live/Registered |
Boston Scientific Scimed, Inc. 2005-10-05 |